Strong LC - Search Results

1

Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation.

Hu Q, Gao F, Tian W, Ruteshouser EC, Wang Y, Lazar A, Stewart J, Strong LC, Behringer RR, Huff V. Hu Q, et al. Among authors: strong lc. J Clin Invest. 2011 Jan;121(1):174-83. doi: 10.1172/JCI43772. Epub 2010 Dec 1. J Clin Invest. 2011. PMID: 21123950 Free PMC article.

2

RNA expression of the WT1 gene in Wilms' tumors in relation to histology.

Miwa H, Tomlinson GE, Timmons CF, Huff V, Cohn SL, Strong LC, Saunders GF. Miwa H, et al. Among authors: strong lc. J Natl Cancer Inst. 1992 Feb 5;84(3):181-7. doi: 10.1093/jnci/84.3.181. J Natl Cancer Inst. 1992. PMID: 1311774

3

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences.

Huff V, Jaffe N, Saunders GF, Strong LC, Villalba F, Ruteshouser EC. Huff V, et al. Among authors: strong lc. Am J Hum Genet. 1995 Jan;56(1):84-90. Am J Hum Genet. 1995. PMID: 7825606 Free PMC article.

4

Genetic mosaicism in normal tissues of Wilms' tumour patients.

Chao LY, Huff V, Tomlinson G, Riccardi VM, Strong LC, Saunders GF. Chao LY, et al. Among authors: strong lc. Nat Genet. 1993 Feb;3(2):127-31. doi: 10.1038/ng0293-127. Nat Genet. 1993. PMID: 8388768

5

Analysis of possible WT1 RNA processing in primary Wilms tumors.

Gunning KB, Cohn SL, Tomlinson GE, Strong LC, Huff V. Gunning KB, et al. Among authors: strong lc. Oncogene. 1996 Sep 19;13(6):1179-85. Oncogene. 1996. PMID: 8808692

6

Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour.

Palculict TB, Ruteshouser EC, Fan Y, Wang W, Strong L, Huff V. Palculict TB, et al. J Med Genet. 2016 Jun;53(6):385-8. doi: 10.1136/jmedgenet-2015-103311. Epub 2015 Nov 13. J Med Genet. 2016. PMID: 26566882 Free PMC article.

7

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors.

McDonald JM, Douglass EC, Fisher R, Geiser CF, Krill CE, Strong LC, Virshup D, Huff V. McDonald JM, et al. Among authors: strong lc. Cancer Res. 1998 Apr 1;58(7):1387-90. Cancer Res. 1998. PMID: 9537236

8

Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.

Huff V, Reeve AE, Leppert M, Strong LC, Douglass EC, Geiser CF, Li FP, Meadows A, Callen DF, Lenoir G, et al. Huff V, et al. Among authors: strong lc. Cancer Res. 1992 Nov 1;52(21):6117-20. Cancer Res. 1992. PMID: 1356625

9

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.

Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF. Huff V, et al. Among authors: strong lc. Am J Hum Genet. 1991 May;48(5):997-1003. Am J Hum Genet. 1991. PMID: 1673293 Free PMC article.

10

Parental origin of de novo constitutional deletions of chromosomal band 11p13.

Huff V, Meadows A, Riccardi VM, Strong LC, Saunders GF. Huff V, et al. Among authors: strong lc. Am J Hum Genet. 1990 Jul;47(1):155-60. Am J Hum Genet. 1990. PMID: 1971994 Free PMC article.

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